CN113372245A - Synthesis method of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine - Google Patents
Synthesis method of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine Download PDFInfo
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- CN113372245A CN113372245A CN202110672313.1A CN202110672313A CN113372245A CN 113372245 A CN113372245 A CN 113372245A CN 202110672313 A CN202110672313 A CN 202110672313A CN 113372245 A CN113372245 A CN 113372245A
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- diethanolamine
- benzoyl
- toluenesulfonyl
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- chloride
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/26—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids
- C07C303/28—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids by reaction of hydroxy compounds with sulfonic acids or derivatives thereof
Abstract
The invention discloses a method for synthesizing N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine, which comprises the following steps: benzoyl chloride, p-toluenesulfonyl chloride and diethanolamine are used as reaction reactants, and the one-pot synthesis of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine is realized by controlling the temperature of two reactions and with high conversion rate and high selectivity. The route of the invention has the advantages of mild reaction conditions, high yield, safety and easy control. In addition, safe and non-combustible dichloromethane is used as a solvent in the route of the invention, so that diethyl ether with extremely high safety risk is avoided, the process safety is greatly improved, and the method is a clean process for industrially producing the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine.
Description
Technical Field
The invention relates to a synthetic method of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine.
Background
N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine, having the molecular structural formula:
N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine, is an important organic ligand intermediate. Can be used for synthesizing ligands such as unsymmetrical substituted 1,4, 7-triazacyclononane, unsymmetrical substituted 1,4,7, 10-tetraza cyclododecane and the like, and is widely applied to the fields of contrast agents, coordination chemical ligands and the like.
The synthesis method of the currently published N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine report comprises the steps of firstly reacting diethanolamine with benzoyl chloride to obtain N-benzoyl diethanolamine, separating the product, and then reacting the product with p-toluenesulfonyl chloride to obtain the final product. U.S. Pat. No. 5,983,338 discloses a process in which diethanolamine and benzoyl chloride are reacted at 0 ℃ in the presence of diethyl ether as solvent to give N-benzoyl-diethanolamine at 90% conversion. US5506224 specifically teaches that recrystallization of the product after the reaction in diethyl ether gives a solid product, and that the applicant repeated the process described in US5506224, always giving only an oily product, no crystalline product and a yield of only about 65%. The traditional synthetic route of the step-by-step method is as follows:
the process uses a large amount of ether which is an easily-prepared poison control chemical in our country and is an extremely dangerous chemical raw material, and the existing process cannot meet the actual industrial production requirements no matter the production cost and the management cost are adopted, or the intrinsic safety in the production process is adopted.
Disclosure of Invention
The invention aims to provide a method for synthesizing N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine, which adopts a one-pot method to obtain the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine through two-step reaction. The invention still takes benzoyl chloride, p-toluenesulfonyl chloride and diethanolamine as reaction reactants, and realizes the one-pot synthesis of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine with high conversion rate and high selectivity by controlling the temperature of two reactions.
The route of the invention has the advantages of mild reaction conditions, high yield, safety and easy control. In addition, safe and non-combustible dichloromethane is used as a solvent in the route of the invention, so that diethyl ether with extremely high safety risk is avoided, the process safety is greatly improved, and the method is a clean process for industrially producing the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine.
The invention aims to realize the synthesis method of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine by the following technical scheme, and the molecular structural formula of the compound is as follows:
the synthesis method comprises the steps of taking benzoyl chloride, p-toluenesulfonyl chloride and diethanolamine as reaction reactants as substrates, taking dichloromethane as a solvent and triethylamine as an acid-binding agent, firstly reacting at a temperature of 80-60 ℃ below zero to generate N-benzoyl diethanolamine, directly adding p-toluenesulfonyl chloride into a system without separation after the reaction is finished, and then reacting at room temperature to generate the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine. The two-step reaction realizes one-pot reaction. The chemical reaction process of the present invention can be expressed by the following formula:
the reaction yield depends on the selectivity of the first step. Besides the reaction of the formula, the benzoyl chloride and the diethanol amine can also undergo an esterification reaction of hydroxyl with the diethanol amine to generate the following three impurities:
the invention controls the reaction temperature between 80 ℃ below zero and 60 ℃ below zero, so that benzoyl chloride reacts with N atoms in diethanolamine molecules in a high selectivity manner to generate N-benzoyl diethanolamine, and then the N-benzoyl diethanolamine and p-toluenesulfonyl chloride react completely at room temperature to obtain the product. Calculated by diethanolamine, the total molar yield of the two-step reaction reaches more than 92 percent, and the product purity reaches more than 99 percent.
Compared with the prior art, the invention has the following beneficial effects: the invention realizes a one-pot method, is simple and convenient to operate, and is safe and controllable; the method avoids ether with extremely high safety risk, greatly improves the process safety, and is a clean process for industrially producing the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine. The one-pot method of the invention unifies the solvents of the two-step reaction, reduces the risks brought by different solvents in industrial production, the total amount of pollutants and the category of pollution factors, and represents the trend of clean production process.
Detailed Description
The invention is further illustrated by the following examples of embodiments.
The N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine has the molecular structural formula:
the synthesis method comprises the steps of taking benzoyl chloride, p-toluenesulfonyl chloride and diethanolamine as reaction reactants as substrates, taking dichloromethane as a solvent and triethylamine as an acid-binding agent, firstly reacting at a temperature of 80-60 ℃ below zero to generate N-benzoyl diethanolamine, directly adding p-toluenesulfonyl chloride into a system without separation after the reaction is finished, and then reacting at room temperature to generate the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine. The two-step reaction realizes one-pot reaction.
The molar ratio of benzoyl chloride to p-toluenesulfonyl chloride to diethanolamine is 1 (2-2.2): 1.
the molar ratio of triethylamine to diethanolamine is (3-4): 1.
The mass ratio of the solvent dichloromethane to the diethanolamine is (20-80): 1.
the reaction temperature is divided into two sections, the first section is between 80 ℃ below zero and 60 ℃ below zero, and the reaction time is 10-24 hours; the second stage reaction temperature is room temperature, and the reaction time is 10-24 hours.
During the specific operation, diethanolamine, triethylamine and dichloromethane are put into a reactor, the temperature is reduced to minus 80 ℃, the dichloromethane solution of benzoyl chloride is dripped into a reaction system, and the dripping speed is controlled, so that the temperature of the reaction system is not more than minus 60 ℃. After the dropwise addition is finished, keeping the temperature for reaction for a certain time, heating to 0-10 ℃, beginning to dropwise add a dichloromethane solution of p-toluenesulfonyl chloride, and controlling the dropwise addition speed to ensure that the temperature of a reaction system is not more than 30 ℃. After the dropwise addition, the reaction mixture is stirred at room temperature for a certain time. After the reaction is completed, direct filtration is carried out, and the filter cake is pulped with water to wash away triethylamine hydrochloride. Pulping, filtering, and drying the filter cake to obtain the N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine.
Example 1
In a 1000ml four-necked flask equipped with an electric stirrer, a thermometer, a dropping funnel and a dry ice acetone bath, 10g (0.095mol) of diethanolamine and 31g (0.31mol) of triethylamine were charged and 100ml of dichloromethane was added, and after stirring was started, the temperature was lowered by the dry ice acetone bath.
Cooling to 80 ℃ below zero, dropwise adding 150ml of dichloromethane solution dissolved with 13.4g (0.095mol) of benzoyl chloride into the reaction system, and controlling the dropwise adding speed so that the temperature of the reaction system is not more than 60 ℃ below zero. After the dropwise addition is finished, keeping the temperature between 70 ℃ below zero and 60 ℃ below zero for reaction for 24 hours, heating to 0-10 ℃, beginning to dropwise add 150ml of dichloromethane solution dissolved with 38g (0.2mol) of p-toluenesulfonyl chloride, and controlling the dropwise adding speed so that the temperature of the reaction system is not more than 30 ℃. After the addition was complete, the mixture was stirred at room temperature overnight. The next day, direct filtration was performed and the filter cake was slurried with water to wash away triethylamine hydrochloride. Pulping, filtering, and drying the filter cake to obtain white powdery N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine. The weight was 46.5 g. The content of the liquid chromatogram is 96.50 percent, and the molar yield is 94.67 percent calculated by diethanolamine.
Example 2
In a 1000ml four-necked flask equipped with an electric stirrer, a thermometer, a dropping funnel and a dry ice acetone bath, 10g (0.095mol) of diethanolamine and 38g (0.38mol) of triethylamine were charged, and after 200ml of dichloromethane was added, stirring was started, and the temperature was lowered with the dry ice acetone bath.
Cooling to 80 ℃ below zero, dropwise adding 150ml of dichloromethane solution dissolved with 13.4g (0.095mol) of benzoyl chloride into the reaction system, and controlling the dropwise adding speed so that the temperature of the reaction system is not more than 60 ℃ below zero. After the dropwise addition is finished, keeping the temperature between 70 ℃ below zero and 60 ℃ below zero for reaction for 24 hours, heating to 0-10 ℃, beginning to dropwise add 150ml of dichloromethane solution dissolved with 40g (0.21mol) of p-toluenesulfonyl chloride, and controlling the dropwise adding speed so that the temperature of the reaction system is not more than 30 ℃. After the completion of the dropwise addition, the mixture was stirred at room temperature for 24 hours. After the reaction is completed, filtration is carried out, and the filter cake is pulped with water to wash away triethylamine hydrochloride. Pulping, filtering, and drying the filter cake to obtain white powdery N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine. The weight was 41 g. The content of liquid chromatography is 99.11%, and the molar yield is 83.47% in terms of diethanolamine.
Claims (5)
1. A synthetic method of N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine comprises the following steps:
the synthesis method is characterized in that benzoyl chloride, p-toluenesulfonyl chloride and diethanolamine are used as reaction reactants, dichloromethane is used as a solvent, triethylamine is used as an acid-binding agent, and N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine is generated through a two-step reaction by a one-pot method;
the reaction equation of the synthesis method is as follows:
2. the method for synthesizing N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine according to claim 1, wherein the molar ratio of benzoyl chloride, p-toluenesulfonyl chloride and diethanolamine is 1 (2-2.2): 1.
3. the method for synthesizing N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine according to claim 1, wherein the molar ratio of triethylamine to diethanolamine is (3-4): 1.
4. The method for synthesizing N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine according to claim 1, wherein the mass ratio of the solvent dichloromethane to diethanolamine is (20-80): 1.
5. the method for synthesizing N-benzoyl-O, O-p-toluenesulfonyl-diethanolamine according to claim 1, wherein the reaction temperature is divided into two stages, the first stage reaction temperature is between 80 ℃ below zero and 60 ℃ below zero, and the reaction time is 10-24 hours; the second stage reaction temperature is room temperature, and the reaction time is 10-24 hours.
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| EP0550006A2 (en) * | 1991-12-31 | 1993-07-07 | LIFEGROUP S.p.A. | Use of N-acyl derivatives of aminoalcohols for the manufacture of a medicament for the treatment of pathologies involving mast cells |
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